CAS: 42346-68-9; 1-Methyl-5-Oxopyrrolidine-3-Carboxylic Acid

该化合物是一种多用途的热循环化合物,其特点是三点方位的有碳酸功能组和一个甲酸功能组的甲基替代体,这种结构具有独特的回活动性,使它作为有机合成和制药应用中的一个构件具有价值. 化合物的极地性质和参与氢联结的能力增强了其在设计生物活性分子或协调金属离子方面的效用. 它在标准条件下的稳定性和与共同合成方法的兼容性进一步有助于其在药用化学和材料科学中的广泛适用性. 碳基和碳基组的存在可以进行多种衍生,能够根据具体的研究或工业需要进行量身定制的修改.

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5733-86-8 428518-42-7 59857-86-2

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上下游产品

CAS号97-65-4 衣康酸 | CAS号74-89-5 氨基甲烷 | CAS号59857-86-2 1-甲基-2-氧代吡咯烷-4-甲酸甲酯 | CAS号617-52-7 衣康酸二甲酯 | CAS号59857-86-2 1-甲基-2-氧代吡咯烷-4-甲酸甲酯 | CAS号19597-07-0 1,3-二甲基吡咯烷-2-酮 | CAS号15542-96-8 1,3-dimethylpyr... | CAS号2555-04-6 1,4-二甲基-2-吡咯烷酮 | CAS号59887-20-6 4-(羟基甲基)-1-甲基吡咯烷-2-酮

合成工艺路线路线简述

    📜1-甲基-5-氧代吡咯烷-3-羧酸甲酯置于sodium Hydroxide体系中,用 甲醇,水 作为反应溶剂,化学反应 24.0H,以91%的收率获得产物1-甲基-2-氧代吡咯烷-4-甲酸
    参考文献:Synthetic Approaches To 10-Azaprostaglandins
    标题:Synthetic Approaches To 10-Azaprostaglandins
    摘要:
    DOI:10.1021/jo01293A010

    海关参考信息

    专利信息


    专利号:US-5879690-A
    优先权日:1995-09-07
    标题:Topical administration of catecholamines and related compounds to subcutaneous muscle tissue using percutaneous penetration enhancers
    发明人:PERRICONE NICHOLAS V
    摘要:Compositions for the topical treatment of sagging subcutaneous muscle and overlying cutaneous tissue contain an active ingredient exhibiting or producing catecholamine activity such as catecholamines and/or related compounds in a dermatologically acceptable carrier that contains at least one percutaneous penetration enhancer. Examplary catecholamines include adrenaline, norepinepherine, dopamine and their precursors; catecholamine precursors such as tyrosine and phenylalanine are preferred. Many embodiments, particularly those employing tyrosine and/or phenylalanine as a catecholamine precursor, further contain a neurotransmitter synthesis enhancer such as dimethylaminoethanol, and other co-factors such as vitamin B 6 and pantothenic acid or calcium pantothenate are included in the composition to enhance the action of the active ingredients. Other compounds that scavenge free radicals and antioxidants may also be added.

    专利号:US-7632519-B2
    优先权日:2005-04-25
    标 题:TRPV1 agonist compounds, formulations, prodrugs, methods for using the same
    发明人:JAMIESON GENE CURTIS; MUHAMMAD NAWEED; BLEY KEITH R
    权利人:NEUROGESX INC
    摘要:Described here are TRPV1 agonist compounds and their methods of synthesis and use. In addition to specifically identified compounds, capsaicin prodrugs, gemini dimers, and mutual prodrugs are also described. Formulations of the TRPV1 agonist compounds may be in the form of a liquid, tablets, capsules, gel, cream, emulsion, a patch, or the like. Methods for treating medical conditions using the compounds, compositions, or prodrugs described, are also provided.

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:Hutskalova, V.; Sparr, C., Science of Synthesis Knowledge Updates, (2022) 1, 29.
    摘要:Chemical and Pharmaceutical Bulletin., 38(2308), 1990 []
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